ClinVar Miner

List of variants in gene KCNB1 reported as benign for not provided

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_004975.4(KCNB1):c.2473C>T (p.Pro825Ser) rs34467662 0.02504
NM_004975.4(KCNB1):c.1847C>G (p.Thr616Ser) rs2229006 0.01543
NM_004975.4(KCNB1):c.1837C>T (p.Pro613Ser) rs112735799 0.01273
NM_004975.4(KCNB1):c.2570G>A (p.Ser857Asn) rs34280195 0.00926
NM_004975.4(KCNB1):c.1182G>A (p.Gly394=) rs77238446 0.00481
NM_004975.4(KCNB1):c.1734G>C (p.Gly578=) rs145456546 0.00081
NM_004975.4(KCNB1):c.2136G>A (p.Thr712=) rs139458439 0.00057
NM_004975.4(KCNB1):c.2363C>A (p.Thr788Lys) rs140932985 0.00045
NM_004975.4(KCNB1):c.1576G>A (p.Val526Ile) rs140932636 0.00034
NM_004975.4(KCNB1):c.2298G>T (p.Leu766=) rs773587323 0.00018
NM_004975.4(KCNB1):c.1356T>C (p.Asp452=) rs775898692 0.00015
NM_004975.4(KCNB1):c.2105C>T (p.Ala702Val) rs144379782 0.00010
NM_004975.4(KCNB1):c.1388T>C (p.Ile463Thr) rs145421532 0.00004
NM_004975.4(KCNB1):c.375C>T (p.Asp125=) rs201414449 0.00004
NM_004975.4(KCNB1):c.2442T>G (p.Ile814Met) rs565025643 0.00003
NM_004975.4(KCNB1):c.2271C>T (p.Asp757=) rs190726852 0.00002
NM_004975.4(KCNB1):c.567+3G>A rs752873604 0.00001
GRCh37/hg19 20q13.13(chr20:47938833-48025102)x3
NM_004975.4(KCNB1):c.1880G>A (p.Arg627Gln) rs754927664

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